List of variants in gene MED25 reported as uncertain significance by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_030973.4(MED25):c.602C>T (p.Pro201Leu)	rs144354024	0.00054
NM_030973.4(MED25):c.679G>A (p.Val227Met)	rs369825113	0.00036
NM_030973.4(MED25):c.1691C>T (p.Ala564Val)	rs750211605	0.00002
NM_030973.4(MED25):c.395G>A (p.Arg132His)	rs1441155267	0.00001
NM_030973.4(MED25):c.1148_1165dup (p.Gln383_Ala388dup)	rs765219800
NM_030973.4(MED25):c.1202C>T (p.Ala401Val)	rs868663771
NM_030973.4(MED25):c.1799G>A (p.Gly600Glu)	rs1188355950
NM_030973.4(MED25):c.23C>A (p.Pro8Gln)	rs980805046
NM_030973.4(MED25):c.249A>C (p.Gln83His)	rs1291395600
NM_030973.4(MED25):c.314G>A (p.Gly105Asp)	rs1281336559
NM_030973.4(MED25):c.377A>T (p.Asp126Val)	rs751058652

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